Schaefer Roland M, Tylki-Szymańska Anna, Hilz Max J
Department of Medicine, University of Muenster, Muenster, Germany.
Drugs. 2009 Nov 12;69(16):2179-205. doi: 10.2165/11318300-000000000-00000.
Fabry disease is a progressive and life-threatening glycolipid storage disorder affecting both males and females. The primary driver of the disease is the accumulation of glycolipids (globotriaosylceramide [GL-3]) in a variety of cell types, including vascular endothelial cells, a range of renal cell types, cardiomyocytes and neurons, which is caused by deficient activity of the lysosomal enzyme, alpha-galactosidase. The disease typically presents during childhood or adolescence. First manifestations reflect involvement of small nerve fibres of the peripheral and autonomic nervous systems. With age, severe complications involving the kidneys, heart and brain cause considerable morbidity and premature death. Outside the US, enzyme replacement therapy (ERT) with agalsidase alfa 0.2 mg/kg every other week (EOW) and agalsidase beta 1.0 mg/kg EOW is available for the treatment of patients with Fabry disease, while agalsidase beta 1.0 mg/kg EOW is the only approved drug in the US. To analyse the evidence for ERT, a systematic review of the literature was performed to identify prospectively designed randomized, controlled trials (RCTs) and open-label studies on the efficacy of agalsidase alfa and agalsidase beta. MEDLINE and EMBASE databases were searched; inclusion criteria for the systematic review were prospectively designed clinical studies evaluating ERT with quantifiable endpoints: double-blind and open-label studies were eligible. Exclusion criteria were review articles, case reports, case studies, letters to the editor and articles based on registry data (Fabry Outcome Survey or Fabry Registry). In addition, any studies with a retrospective design or data based on post hoc analyses were excluded. The evidence was reviewed with respect to the clinical benefits of ERT at the level of the end organ. A total of 9 RCTs and 23 open-label studies were identified for inclusion. The efficacy of ERT in Fabry disease has been measured against a variety of endpoints, the majority of which were subclinical parameters rather than clinical outcomes. Plasma levels of GL-3 together with accumulation in the kidney, heart and skin were the most commonly studied endpoints, followed by renal endpoints of proteinuria and glomerular filtration rate, whereas cardiac and neurological endpoints were not commonly studied. To date, only one RCT with ERT defined hard clinical outcomes in the form of cardiac, renal or cerebrovascular events, or death as its primary endpoint. The currently available data from prospective RCTs and open-label studies in patients with Fabry disease are more robust for ERT at a dose of 1 mg/kg EOW than a dose of 0.2 mg/kg EOW, although the beneficial effects of ERT with either dose or preparation are variable.
法布里病是一种进行性且危及生命的糖脂贮积病,男性和女性均可患病。该疾病的主要驱动因素是糖脂(Globotriaosylceramide [GL-3])在多种细胞类型中蓄积,包括血管内皮细胞、多种肾细胞类型、心肌细胞和神经元,这是由溶酶体酶α-半乳糖苷酶活性不足所致。该疾病通常在儿童期或青春期出现。最初的表现反映了外周和自主神经系统的小神经纤维受累。随着年龄增长,涉及肾脏、心脏和大脑的严重并发症会导致相当高的发病率和过早死亡。在美国以外地区,每两周一次给予阿加糖酶α 0.2 mg/kg和每两周一次给予阿加糖酶β 1.0 mg/kg的酶替代疗法(ERT)可用于治疗法布里病患者,而每两周一次给予阿加糖酶β 1.0 mg/kg是美国唯一获批的药物。为分析ERT的证据,对文献进行了系统综述,以确定前瞻性设计的随机对照试验(RCT)以及关于阿加糖酶α和阿加糖酶β疗效的开放标签研究。检索了MEDLINE和EMBASE数据库;系统综述的纳入标准是前瞻性设计的临床研究,评估具有可量化终点的ERT:双盲和开放标签研究均符合条件。排除标准为综述文章、病例报告、病例研究、给编辑的信件以及基于注册数据(法布里病结局调查或法布里病注册)的文章。此外,任何具有回顾性设计或基于事后分析的数据的研究均被排除。从终末器官层面审查了ERT临床益处的证据。共确定9项RCT和23项开放标签研究纳入分析。ERT在法布里病中的疗效已根据多种终点进行衡量,其中大多数是亚临床参数而非临床结局。血浆GL-3水平以及在肾脏、心脏和皮肤中的蓄积是最常研究的终点,其次是蛋白尿和肾小球滤过率的肾脏终点,而心脏和神经终点则较少被研究。迄今为止,仅有一项ERT的RCT将心脏、肾脏或脑血管事件形式的硬性临床结局或死亡作为其主要终点。法布里病患者前瞻性RCT和开放标签研究的现有数据表明,每两周一次给予1 mg/kg剂量的ERT比每两周一次给予0.2 mg/kg剂量的ERT更有效,尽管两种剂量或制剂的ERT的有益效果存在差异。